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Fractures, Bone clinical trials

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NCT ID: NCT00323609 Terminated - Clinical trials for Vertebral Body Compression Fractures

KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restoration of Vertebral Body Compression Fractures

Start date: August 2006
Phase: N/A
Study type: Interventional

Patients with osteoporotic vertebral body compression fractures will be randomly assigned to treatment with balloon kyphoplasty or vertebroplasty. Over 2 years of follow-up, back pain, back function, quality of life, adverse events, subsequent fractures and cumulative healthcare costs will be compared.

NCT ID: NCT00323232 Completed - Hip Fracture Clinical Trials

Comparison of Treatment Outcomes in Hip Fractures Surgically Fixed With Either a Two or Four Hole Device.

Start date: December 2010
Phase: Phase 4
Study type: Interventional

Although Standard of Care for Hip Fractures is the Device (Dynamic Hip Screw) being studied in this project, and both sizes (the 2 and the 4 hole versions) are currently in use there is not widespread agreement yet whether there is an optimal number of screws (2 or 4) required for the best outcomes. If it can be shown that a 2 hole version is just as successful in outcomes it would allow for a smaller incision (surgical cut) at the site of the fracture. This could reduce soft tissue dissection, operating time, and surgical blood loss. This in turn would reduce post operative pain, blood loss, and hospital length of stay.

NCT ID: NCT00317837 Withdrawn - Clinical trials for Femoral Neck Fractures

Bipolar Versus Unipolar Hemiarthroplasty for Patients With a Hip Fracture

Start date: October 2004
Phase: N/A
Study type: Interventional

Insertion of a hemiarthroplasty is a well established treatment for a dislocated medial hip fracture in elderly patients. The purpose of this study is to compare unipolar and bipolar hemiarthroplasty as a treatment for patients aged 70 years or above with a dislocated medial femoral neck fracture. The study is prospective and randomised, and will be based on questionnaires, clinical examinations, registration of complications and radiographic evaluation at follow up at 3 months, 1 and 3 years postoperatively.

NCT ID: NCT00314600 Recruiting - Fracture Clinical Trials

Treatment of Non-Dislocated Midshaft Both-Bone Fractures

Start date: January 2006
Phase: N/A
Study type: Interventional

The investigators created a randomized clinical trial to find out what kind of treatment is optimal for non-dislocated both-bone midshaft forearm fractures.

NCT ID: NCT00314587 Recruiting - Fracture Clinical Trials

Treatment of Unstable Both-Bone Midshaft Forearm Fractures in Children

Start date: January 2006
Phase: N/A
Study type: Interventional

The investigators created a randomized clinical trial between 1 or 2 elastic stable intramedullary nails to find out what kind of treatment is optimal for unstable both-bone midshaft forearm fractures.

NCT ID: NCT00307905 Withdrawn - Pain Clinical Trials

TRAUMEEL for Pain After Fracture of Neck of Femur

Start date: January 2011
Phase: Phase 3
Study type: Interventional

We hypothesize that Traumeel S is more effective than placebo in reducing 48-hour mean cumulative morphine consumption in patients scheduled for surgical correction of fracture of neck of hip. 224 patients, meeting all inclusion and none of exclusion criteria, will be enrolled in the trial. Patients will be randomized to receive either intraoperative injection and post operative oral Traumeel S Tablets or placebo injection (normal saline) and indistinguishable oral placebo tablets. Baseline measurements of relevant outcome measures will taken preoperatively. Immediately after surgery, patients will receive an initial dose of morphine of 0.1mg/kg body weight. Patients will take the oral study medication for 21 days. Every four hours after surgery, patients will be asked to grade their pain on an NRS. Subsequent doses of morphine will be calculated based upon the patient's weight and current NRS, according to a preplanned scheme. Patients will be permitted to request additional morphine, beyond their calculated dose.

NCT ID: NCT00299052 Completed - Open Fracture Clinical Trials

Efficacy of DBM on Fractures of the Shinbone (Tibia)

Start date: March 2006
Phase: Phase 4
Study type: Interventional

The Tibia bone (shinbone) is located in the leg, itis the most frequently fractured bone in the body and has very poor blood supply because it is surrounded by skin and fat instead of muscle like the thighbone causing healing problems. Problems frequently found during the healing process are malunion (bone heals in the wrong place), nonunion (the bone never heals), and compartment syndrome (a big inflammation of muscle that causes compression of nerves and blood vessels) with necrosis (death) of tissue. Surgeons have tried to decrease these problems by using different surgical techniques and substances to accelerate healing. Substances frequently used in fractures are bone grafts. Bone grafts are normally obtained from the wrist or the hip bone, and sometimes can cause other complications varying from pain to infection. To avoid complications, investigators have used alternatives such as obtaining bone from donors. The donor bone grafts are carefully analyzed and cleaned to ensure they will not cause problems for the receiver. Bone obtained from donors is called Demineralized Bone Matrix (DBM). DBM has proved to be very effective in helping fractures to heal faster and we want to use it in patients with tibia fractures. This study is important because DBM can improve the way tibia fractures are treated and could have the potential to decrease the time patients must stay in the hospital. DBM could improve healing time and diminish overall costs. Also, with the use of DBM plus reamings, patients will have fewer complications like pain and infection.

NCT ID: NCT00293189 Recruiting - Hip Fracture Clinical Trials

Gene-Polymorphies in the P2X7 Gene in Patients With Osteoporotic Fractures

Start date: December 2005
Phase: N/A
Study type: Observational

We are looking after gene-polymorphies in the p2x7-gene in patient with osteoporotic fractures.

NCT ID: NCT00292006 Withdrawn - Fracture Clinical Trials

Computerized Tomography to Help Diagnosis Pediatrics Scaphoid Fractures.

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find out whether computerized tomography will be better than plain radiographs in determining pediatrics scaphoid fractures.

NCT ID: NCT00290862 Unknown status - Spinal Fractures Clinical Trials

A Safety and Efficacy Study for Treatment of Painful Vertebral Compression Fractures Caused by Osteoporosis

Start date: September 2004
Phase: N/A
Study type: Interventional

Doctors are studying an investigational treatment to be used during the vertebroplasty procedure when treating vertebral compression fractures (spine fractures) that may help to reduce pain and restore mobility. If one has experienced back pain for at least 4 weeks but not longer than 1 year, he/she may be eligible to participate. The purpose of this protocol is to describe the methods for the clinical evaluation of Cortoss for vertebroplasty in patients with painful osteoporotic compression fractures. Eligible patients with painful osteoporotic compression fractures of the spine are divided into two groups. Each enrolled patient will have the vertebroplasty procedure; however one group of patients will have the vertebroplasty procedure using polymethylmethacrylate [PMMA] (a Food and Drug Administration [FDA]-approved bone cement) and the other group of patients will have the vertebroplasty procedure using a relatively new (investigational) biomaterial called Cortoss.